HPV Mutation Detail Information

> A7689G Search Result


Mutation Information
Mutation Site A7689G
Mutation Type Nucleotide level
Gene/Protein/Region Type E7
Nucleotide_Mutation N29S
Genotype/Subtype HPV16
Viral Reference NC_001526
Country China
Literature Information
PubMed PMID 31670402
Disease Cervical intraepithelial neoplasia
Published Year 2020
Journal Journal of medical virology
Title Genetic variability and functional implication of HPV16 from cervical intraepithelial neoplasia in Shanghai women.
Author Zhao J,Zhu J,Guo J,Zhu T,Zhong J,Liu M,Ruan Y,Liao S,Li F
Evidence In the 21 nucleotide variations of the E6 and E7 sequences, the frequency of T7220G and A7689G were the highest, which caused amino acid mutations (D32E and N29S).

Contents
Description
Mutation Information Note
  • Gene/Protein/Region Type: Virus Gene (e.g. LMP-1) or Virus Protein (e.g. Rep 68) or Virus Region (e.g. S, X)
Literature Information Note
  • Evidence: sentence contains this mutation information in the citation